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"Medtronic" Zhu Keli calibration accessory (unsterilized) - Taiwan Registration f3bf50fa10ee568e253fd988b9615a4a

Access comprehensive regulatory information for "Medtronic" Zhu Keli calibration accessory (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f3bf50fa10ee568e253fd988b9615a4a and manufactured by SMITH & NEPHEW INC., ENDOSCOPY DIVISION. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Covidien llc;; Viant AS&O Holdings, LLC, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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f3bf50fa10ee568e253fd988b9615a4a
Registration Details
Taiwan FDA Registration: f3bf50fa10ee568e253fd988b9615a4a
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Device Details

"Medtronic" Zhu Keli calibration accessory (unsterilized)
TW: "็พŽๆ•ฆๅŠ›" ็ฅๅฏ้บ—ๆ กๆบ–้™„ไปถ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

f3bf50fa10ee568e253fd988b9615a4a

DHA09401841407

Company Information

Product Details

Limited to the first level identification range of the medical device management measures "hysteroscopic perfusion device (L.1700)".

l Obstetrics and Gynecology

L.1700 ๅญๅฎฎ้ก็Œๅ…ฅๅ™จ

import

Dates and Status

Oct 17, 2017

Oct 17, 2022

Apr 12, 2024

Cancellation Information

Logged out

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